| Tag | Content |
|---|
EnhancerAtlas ID | HS060-03467 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr10:11484300-11485580 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr10:11485090-11485101 | TCCTGTTTACA | + | 6.62 | | IRF1 | MA0050.2 | chr10:11485147-11485168 | TGTCACTTTCTCTTTTTGTGT | + | 6.18 | | IRF1 | MA0050.2 | chr10:11485141-11485162 | TTTGACTGTCACTTTCTCTTT | + | 6.27 | | NEUROG2 | MA0669.1 | chr10:11484960-11484970 | GACATATGTT | - | 6.02 | | NFIL3 | MA0025.1 | chr10:11485181-11485192 | TTATGTAACAT | + | 6.32 | | SOX10 | MA0442.2 | chr10:11484775-11484786 | AAAACAAAGAA | + | 6.62 | | STAT1 | MA0137.3 | chr10:11484753-11484764 | TTTCTAGGAAA | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCCTGAGTT TTGTGAGCCA CTCTAGCAAA TTAACCGAAC CCAAGAAGGG AGTCGTGGGA 60
ACCCTGATTT ATAGCTGGTC ACTGAGAAGC ACAGATAGAG CCACCTGGGG CTTGCGATTG 120
GCAGCAGGAG TGGGGACAGA GTCTTGTGGA CTGAGTCCTC AGCCTGTGGG ATCTGACGCT 180
ACCTCTGGGT AGTGTCAATA GCGTCAGAAT TGAATTGGAT TGCAGGACAC CCAACTGGTG 240
TCTCTGCAGA ACTGACGGCT TGCACATTGG CGTGCAGTGG AGAAAACCCC ACCCACACAG 300
AGGTCTTCTG TGTTGATCAT TGTGGTGCGA GAGCAGAGAA AAAACAGTTT TGAGTTTTTT 360
GGACTCACCT TAGCACCATC ATAAAGTCAG GGACCATCTA CATTTTCAGA GTGTTGCAAA 420
CAGATTTTTT TGTTAAAGTA CTCAAAACAT TAATTTCTAG GAAAACAGGA TTCATAAAAC 480
AAAGAAATGC AACCCCCCCA CTTTATGATT AAATTCAAAA AATATGAAAA TTAGTCTGCC 540
AAATGCTTTA AAAGTTCTCA AAACCTTACT CTCAATTTCT GAACTTACCT CTTCGCAGAC 600
GTGTAGCAAC CAGTCCCCCA GGTGGCCCCA GGTCACGGGC TACAAGTTGA GTGGCTCTAA 660
GACATATGTT ACCACCGGAG CACTCTTCAC CCAAGAAGAT CATGGAAACA CAGGTCAAAT 720
AAGGTGTGGA AAACACCACG TATAGTTTTG GACGTGCACA GCGAGGCAGC ATATTGAAGG 780
TGCTGAGAAG TCCTGTTTAC AACAAAAACA GAAATCTGCT CACCTTTGCT CAGTTTCCAA 840
ATTTGACTGT CACTTTCTCT TTTTGTGTTT ACTTATTATT TTTATGTAAC ATTGCAACAT 900
TTGCCAAACC CCATTCCACC AAGAAATGCT TGCCTGGCCT CATGGGAACC TGCTCAGCCT 960
GGCAGAAGGA AGTCACTAAT TCTGAAACCT AAGGTCCGGG TCAGGCCCGA GGTGGCGATG 1020
CCTGGAGCCA GGCGCACCAA GCAGTGCAGG CAATCGCTTC AGGTGAAACT CAGTTTCCTC 1080
TTTATTTGCT TTGCTGCAGT GAATAAGAAC CCCAGCTGTT ACTGTTACTG CAACTTGGCC 1140
ATTGCCTGGC ACGTGGGGCC GCGTGGCCGT TAAGAAAAGT CTGCGCACAG AATACACTCA 1200
TTTGAGTGTA AGGAGACCAC GCGTTGCATC AGGGAGCTCC AGCGCACCAG GAAGAGCGAC 1260
ACTGTTTATC CCTCCCCCAG 1280
|
| |
|
|
|
